CorVascular
CorVascular has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jan 8, 2026 · NAI
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 1 | Nov 13, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jan 8, 2026 | Minnetonka, MN | Devices | No Action Indicated (NAI) | 3033275035 |
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3033275035 | Minnetonka, MN | 1 | Jan 8, 2026 |
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